Novel pharmaceutical salts and polymorphs of a factor Xa inhibitor

ABSTRACT

The present invention provides for salts comprising a compound of Formula I and an acid that has activity against mammalian factor Xa. The present invention is also directed to methods of making the compound of Formula I.

CROSS-REFERENCES TO RELATED APPLICATIONS

This application claims the benefit under 35 U.S.C. §119(e) of U.S.Provisional Application Ser. No. 60/735,224 filed Nov. 8, 2005, which ishereby incorporated by reference in its entirety.

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention is directed to novel salts of a factor Xa inhibitor,polymorphs thereof and methods of making the factor Xa inhibitor.

2. State of the Art

Hemostasis, the control of bleeding, occurs by surgical means, or by thephysiological properties of vasoconstriction and coagulation. Thisinvention is particularly concerned with blood coagulation and ways inwhich it assists in maintaining the integrity of mammalian circulationafter injury, inflammation, disease, congenital defect, dysfunction, orother disruption. Although platelets and blood coagulation are bothinvolved in restoring hemostasis and in thrombotic diseases, certaincomponents of the coagulation cascade are primarily responsible for theamplification and acceleration of the processes involved in plateletaggregation and fibrin deposition which are major events in thrombosisand hemostasis.

Clot formation involves the conversion of fibrinogen to fibrin whichpolymerizes into a network to restore hemostasis after injury. A similarprocess results in occluded blood vessels in thrombotic diseases. Theconversion of fibrinogen to fibrin is catalyzed by thrombin, the endproduct of a series of reactions in the blood coagulation cascade.Thrombin is also a key player in activating platelets, therebycontributing to thrombosis under conditions of both arterial and venousblood flow. For these reasons, it has been postulated that efficientregulation of thrombin can lead to efficient regulation of thrombosis.Several classes of currently used anticoagulants directly or indirectlyaffect thrombin (i.e. unfractionated heparins, low-molecular weightheparins, heparin-like compounds, pentasaccharide and warfarin). Director indirect inhibition of thrombin activity has also been the focus of avariety of anticoagulants in clinical development (reviewed by Erikssonand Quinlan, Drugs 11: 1411-1429, 2006).

Prothrombin, the precursor for thrombin, is converted to the activeenzyme by factor Xa. Localized activation of tissue factor/factor VIIamediated factor Xa generation is amplified by the factor IXa/factorVIIIa complex and leads to prothrombinase assembly on activatedplatelets. Factor Xa, as a part of the prothrombinase complex, is thesole enzyme responsible for sustained thrombin formation in thevasculature. Factor Xa is a serine protease, the activated form of itsprecursor Factor X, and a member of the calcium ion binding, gammacarboxyglutamic acid (GLA)-containing, vitamin K dependent, and bloodcoagulation factors. Unlike thrombin, which acts on a variety of proteinsubstrates including fibrinogen and the PAR receptors (Proteaseactivated receptors, Coughlin, J. Thrombosis Haemostasis 3: 1800-1814,2005), factor Xa appears to have a single physiologic substrate, namelyprothrombin. Since one molecule of factor Xa may be able to generategreater than 1000 molecules of thrombin (Mann, et al., J. Thrombosis.Haemostasis 1: 1504-1514, 2003), direct inhibition of factor Xa as a wayof indirectly inhibiting the formation of thrombin may be an efficientanticoagulant strategy. This assertion is based on the key role ofprothrombinase in thrombin synthesis and on the fact that inhibition ofprothrombinase will have a pronounced effect on the overall plateletaggregation and clotting pathways.

Activated proteases such as factor VIIa, factor IXa or factor Xa havepoor proteolytic activity on their own. However, their assembly intocofactor-dependent, membrane-bound complexes significantly enhancestheir catalytic efficiencies. This effect is most dramatic for factorXa, where the efficiency is increased by a factor of 10⁵ (Mann, et al.,Blood 76(1):1-16, 1990). Due to the higher concentration of the zymogenspresent in blood (1.4 μM prothrombin versus 150 nM factor Xa) and thekinetics of activation, a smaller amount of factor Xa than thrombinneeds to be inhibited to achieve an anticoagulant effect. Indirect proofof the hypothesis of superiority of factor Xa as a therapeutic targetcompared to thrombin can also be found in clinical trials for theprevention of deep vein thrombosis. Fondaparinux, an antithrombin IIIdependent factor Xa inhibitor, was proven to be superior to enoxaparin(a low molecular weight heparin that inhibits both thrombin and factorXa) in four trials of orthopedic surgery (Turpie, et al., ArchivesInternal Medicine 162(16): 1833-1840, 2002). Therefore, it has beensuggested that compounds which selectively inhibit factor Xa may beuseful as in vitro diagnostic agents, or for therapeutic administrationin certain thrombotic disorders, see e.g., WO 94/13693.

Several factor Xa inhibitors have been reported as polypeptides derivedfrom hematophagous organisms, as well as compounds which are not largepolypeptide-type inhibitors. Additional factor Xa inhibitors includesmall molecule organic compounds, such as nitrogen containingheterocyclic compounds which have amidino substituent groups, whereintwo functional groups of the compounds can bind to factor Xa at two ofits active sites. For example, WO 98/28269 describes pyrazole compoundshaving a terminal amidino (—C(═NH)—NH₂) group; WO 97/21437 describesbenzimidazole compounds substituted by a basic radical which areconnected to a naphthyl group via a straight or branched chain alkylene,—C(═O)— or —S(═O)₂— bridging group; WO 99/10316 describes compoundshaving a 4-phenyl-N-alkylamidino-piperidine and4-phenoxy-N-alkylamidino-piperidine group connected to a 3-amidinophenylgroup via a carboxamidealkyleneamino bridge; and EP 798295 describescompounds having a 4-phenoxy-N-alkylamidino-piperidine group connectedto an amidinonaphthyl group via a substituted or unsubstitutedsulfonamide or carboxamide bridging group.

Additional reported factor Xa inhibitors include those having astructure comprising a phenyl-amidino, phenyl, and halo-phenyl connectedvia amide linkages (U.S. Pat. No. 6,844,367 B1). Other factor Xainhibitors have replaced the halo-phenyl with a halo-pyridyl (see U.S.Pat. Nos. 6,376,515 B2 and 6,835,739 B2). U.S. Pat. No. 6,376,515 B2discloses a specific factor Xa inhibitor compound identified in Example206, which is also disclosed in U.S. Pat. No. 6,835,739 B2 as Example206 and herein identified as a compound of Formula I. The compound ofFormula I is represented by the structure:

Further work in developing selective inhibitors of factor Xa has led tothe surprising discovery that certain salts of this compound exhibitbetter thermal and hydrolytic stability than the free-base compoundsthemselves or other salts, with the maleate salt having the beststability observed.

SUMMARY OF THE INVENTION

In one embodiment, the invention is directed to a salt comprising acompound Formula I:

and an acid, wherein the acid is selected from the group consisting ofhydrochloric, lactic, maleic, phenoxyacetic, propionic, succinic,adipic, ascorbic, camphoric, gluconic, phosphic, tartric, citric,methanesulfonic, fumaric, glycolic, naphthalene-1,5-disulfonic, gentisicand benzenesulfonic.

In a preferred embodiment, the acid is selected from the groupconsisting of hydrochloric, lactic, maleic, phenoxyacetic, propionic,succinic, adipic, ascorbic, camphoric, gluconic, phosphic, tartric,citric, and methanesulfonic.

In another preferred embodiment, the acid is selected from the groupconsisting of hydrochloric, lactic, maleic, phenoxyacetic, propionic,and succinic. In one embodiment, the salt is the maleate salt or thepropionate salt. It is contemplated that the maleate salt of thecompound of Formula I could be formed by protenating one or morenitrogen atoms of the compound of Formula I. In one embodiment, theamidino nitrogen (═NH) of Formula I is protenated (═NH₂ ⁺) to form thesalt.

In one preferred embodiment, the maleate salt of the compound of FormulaI is represented by Formula II:

In another embodiment, the present invention provides a salt of FormulaII having a crystalline polymorph form. In preferred embodiments, thecrystalline polymorph form exhibits a powder X-ray diffraction patternhaving at least four and more preferably eight of the followingapproximate characteristic peak locations: 4.9, 9.7, 13.8, 14.1, 15.2,17.6, 18.5, 20.8, 21.6, 22.7, 24.1, 26.3, 26.8 degrees 2θ. In stillanother embodiment, the powder X-ray diffraction pattern has approximatecharacteristic peak locations of 4.9, 9.7, 11.8, 13.8, 14.1, 15.2, 17.6,18.5, 19.9, 20.8, 21.6, 22.7, 24.1, 25.0, 26.3, 26.8 degrees 2θ. Theinvention contemplates that the approximate characteristic peaks willhave a deviation of up to about ±0.2 degrees 2θ. In yet anotherembodiment, the powder X-ray diffraction pattern is approximate to thepowder X-ray diffraction pattern shown in FIG. 1. In other embodiments,the present invention provides a salt of Formula II having a crystallinepolymorph form having a differential scanning calorimetry patternapproximate to the differential scanning calorimetry pattern shown inFIG. 2. This crystalline polymorph of the salt of Formula II providesfor a reproducible form of this compound suitable for clinical studies.

In a further embodiment, the present invention provides a pharmaceuticalcomposition for preventing or treating a condition in a mammalcharacterized by undesired thrombosis comprising a pharmaceuticallyacceptable carrier and a therapeutically effective amount of a saltcomprising the compound of Formula I, the maleate salt of the compoundof Formula I, the salt of Formula II, or the salt of Formula II having acrystalline polymorph form. In another embodiment, the pharmaceuticalcomposition is in tablet form. In yet another embodiment, thepharmaceutical composition is in capsule form. In still anotherembodiment, the pharmaceutical composition is in lozenge form. In otherembodiments, the pharmaceutical composition is in a form suitable forinfusion, injection, or transdermal delivery.

In some embodiments, the present invention provides a method forpreventing or treating a condition in a mammal characterized byundesired thrombosis comprising administering to the mammal atherapeutically effective amount of a salt comprising the compound ofFormula I, the maleate salt of the compound of Formula I, the salt ofFormula II, or the salt of Formula II having a crystalline polymorphform. In another embodiment, the condition is selected from the groupconsisting of acute coronary syndrome, myocardial infarction, unstableangina, refractory angina, occlusive coronary thrombus occurringpost-thrombolytic therapy or post-coronary angioplasty, a thromboticallymediated cerebrovascular syndrome, embolic stroke, thrombotic stroke,transient ischemic attacks, venous thrombosis, deep venous thrombosis,pulmonary embolus, coagulopathy, disseminated intravascular coagulation,thrombotic thrombocytopenic purpura, thromboanglitis obliterans,thrombotic disease associated with heparin-induced thrombocytopenia,thrombotic complications associated with extracorporeal circulation,thrombotic complications associated with instrumentation, and thromboticcomplications associated with the fitting of prosthetic devices.

In another embodiment, the present invention provides a method forinhibiting the coagulation of a blood sample comprising the step ofcontacting the sample with a salt comprising the compound of Formula I,the maleate salt of the compound of Formula I, the salt of Formula II,or the salt of Formula II having a crystalline polymorph form.

In a further embodiment, the present invention provides a method ofpreparing a compound of Formula I comprising contacting LiN(CH₃)₂ with acompound of formula III:

or a salt thereof under conditions to form the compound of Formula I.

In some embodiments, the conditions are nucleophilic addition conditionsand comprise use of a non-polar, aprotic solvent. In some otherembodiments, the solvent is a member selected from the group consistingof tetrahydrofuran, diethyl ether, dimethoxymethane, dioxane, hexane,methyl tert-butyl ether, heptane, and cyclohexane. In some embodiments,the salt of the compound of Formula III is the HCl salt.

In some embodiments, the present invention provides a method ofpreparing a compound of Formula I wherein the method is performed at atemperature of less than 10° C.

In a further embodiment, the present invention provides a method ofpreparing a compound of Formula I wherein the compound having Formula Iis afforded in a yield of at least 50%. In another embodiment, thecompound having Formula I is afforded in a yield of at least 65%. Instill another embodiment, the compound having Formula I is afforded in ayield of at least 75%.

In another embodiment, the present invention provides a method of makingthe compound of Formula I on a gram scale or a kilogram scale.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A and 1B provide an X-ray powder diffraction (XRPD) of a form ofFormula II (a maleate salt). FIG. 1A shows the observed diffractionpattern while FIG. 1B shows a calculated diffraction pattern.

FIGS. 2A and 2B provide the differential scanning calorimetry (DSC) andthermal gravimetric analysis (TGA) data, respectively, of the maleatesalt of Formula II.

FIG. 3 provides the gravimetric water sorption (GVS) data of the maleatesalt of Formula II.

FIG. 4 provides two views of a molecule of the maleate salt of FormulaII from the crystal structure data showing the numbering schemeemployed. Anisotropic atomic displacement ellipsoids for thenon-hydrogen atoms are shown at the 50% probability level. Hydrogenatoms are displayed with an arbitrarily small radius.

DETAILED DESCRIPTION OF THE INVENTION

As discussed in U.S. Pat. No. 6,376,515 B2, a compound of Formula I is apotent factor Xa inhibitor. However, the compound of Formula I did notexhibit optimum solubility or crystallinity. The preparation of theacetate salt of the compound of Formula I was found to have goodcrystallinity, but did not possess good thermal and hydrolyticstability. Surprisingly and unexpectedly, it was found that certainsalts show good crystallinity and thermal and hydrolytic stability,including; by way of example, HCl salt, lactate, maleate,phenoxyacetate, propionate, succinate, adipate, ascorbate, camphorate,gluconate, phosphate, tartrate, citrate, mesylate, fumarate, glycolate,naphthalene-1,5-disulphonate, gentisate and benzene sulfonate.

In particular, the maleate salt of Formula II exhibits excellentcrystallinity, thermal and hydrolytic stability and purity. The maleatesalt of Formula II of the present invention is useful for the treatmentof undesired thrombosis in mammals.

I. DEFINITIONS

As used herein, the term “polymorph” refers to the crystalline form of asubstance that is distinct from another crystalline form but that sharesthe same chemical formula.

The term “treatment” or “treating” means any treatment of a disease ordisorder in a subject, such as a mammal, including:

preventing or protecting against the disease or disorder, that is,causing the clinical symptoms not to develop;

inhibiting the disease or disorder, that is, arresting or suppressingthe development of clinical symptoms; and/or

relieving the disease or disorder that is, causing the regression ofclinical symptoms.

As used herein, the term “preventing” refers to the prophylactictreatment of a patient in need thereof. The prophylactic treatment canbe accomplished by providing an appropriate dose of a therapeutic agentto a subject at risk of suffering from an ailment, thereby substantiallyaverting onset of the ailment.

It will be understood by those skilled in the art that in humanmedicine, it is not always possible to distinguish between “preventing”and “suppressing” since the ultimate inductive event or events may beunknown, latent, or the patient is not ascertained until well after theoccurrence of the event or events. Therefore, as used herein the term“prophylaxis” is intended as an element of “treatment” to encompass both“preventing” and “suppressing” as defined herein. The term “protection,”as used herein, is meant to include “prophylaxis.”

The term “therapeutically effective amount” refers to that amount of asalt of this invention, typically delivered as a pharmaceuticalcomposition, that is sufficient to effect treatment, as defined herein,when administered to a subject in need of such treatment. Thetherapeutically effective amount will vary depending upon the subjectand disease condition being treated, the weight and age of the subject,the severity of the disease condition, the particular compound chosen,the dosing regimen to be followed, timing of administration, the mannerof administration and the like, all of which can be determined readilyby one of ordinary skill in the art.

As used herein, the term “condition” refers to a disease state for whichthe compounds, salts, compositions and methods of the present inventionare being used against.

As used herein, the term “blood sample” refers to whole blood taken froma subject, or any fractions of blood including plasma or serum.

II. POLYMORPHIC COMPOUNDS

One embodiment of the invention is a salt comprising the compound ofFormula I. One of skill in the art will appreciate that other salts ofthe free base of Formula I are also useful in the present invention.These other salts can be prepared using inorganic and organic acidswhich provide the requisite thermal and hydrolytic stability, such as,but not limited to, hydrochloric, lactic, maleic, phenoxyacetic,propionic, succinic, adipic, ascorbic, camphoric, gluconic, phosphic,tartric, citric, methanesulfonic, fumaric, glycolic,naphthalene-1,5-disulfonic, gentisic and benzenesulfonic. In oneembodiment, the maleate salt of Formula II is represented as:

The salts of the present invention, such as the salt of Formula II, canadopt several different crystalline forms. The ability of a singlecompound to adopt one of many crystalline forms is termed polymorphism.A crystalline polymorph of a given compound is chemically identical toany other crystalline polymorph of that compound in containing the sameatoms bonded to one another in the same way, but differs in its crystalforms. The different crystalline forms of the same compound can have animpact one or more physical properties, such as stability, solubility,melting point, bulk density, flow properties, bioavailability, etc.

Polymorphs can be characterized by their crystalline structure (X-raydiffraction pattern), their thermal properties (as determined by DSC andTGA), stability, solubility, etc. The X-ray diffraction pattern ispresented as charasteristic peaks ±0.2 degrees 2θ. One polymorph of thesalt of Formula II is characterized by the X-ray diffraction patternshown in FIGS. 1A and 1B, the DSC/TGA data shown in FIGS. 2A and 2B, andthe water sorption data shown in FIG. 3 or combinations of two of thesecharacteristics or all of these characteristics. One of skill in the artwill appreciate that other polymorphs of the salt of Formula II are alsouseful in the present invention.

III. PHARMACEUTICAL COMPOSITIONS

The pharmaceutical compositions of the present invention can be used forpreventing or treating a subject suffering from a condition, wherein thecondition is characterized by undesired thrombosis. The pharmaceuticalcompositions of the present invention are comprised of apharmaceutically acceptable carrier and a therapeutically acceptableamount of a salt comprising the compound of Formula I, the maleate saltof the compound of Formula I, the salt of Formula II, or the salt ofFormula II having a crystalline polymorph form.

A. Pharmaceutically Acceptable Carriers

Diagnostic applications of the saltsof this invention will typicallyutilize formulations such as solutions or suspensions.

In the management of thrombotic disorders the salts of this inventionmay be utilized in compositions such as tablets, capsules, lozenges orelixirs for oral administration, suppositories, sterile solutions orsuspensions or injectable administration, and the like, or incorporatedinto shaped articles. Subjects in need of treatment (typically mammaliansubjects) can be administered appropriate dosages of the compounds ofthis invention that will provide optimal efficacy. The dose and methodof administration will vary from subject to subject and be dependentupon such factors as the type of mammal being treated, its sex, weight,diet, concurrent medication, overall clinical condition, the particularsalts employed, the specific use for which these salts are employed, andother factors which those skilled in the medical arts will recognize.

Capsules useful in the present invention can be prepared usingconventional and known encapsulation techniques, such as that describedin Stroud et al., U.S. Pat. No. 5,735,105. The capsule is typically ahollow shell of generally cylindrical shape having a diameter and lengthsufficient so that the pharmaceutical solution compositions containingthe appropriate dose of the active agent fits inside the capsule. Theexterior of the capsules can include plasticizer, water, gelatin,modified starches, gums, carrageenans, and mixtures thereof. Thoseskilled in the art will appreciate what compositions are suitable.

In addition to the active agent, tablets useful in the present inventioncan comprise fillers, binders, compression agents, lubricants,disintegrants, colorants, water, talc and other elements recognized byone of skill in the art. The tablets can be homogeneous with a singlelayer at the core, or have multiple layers in order to realize preferredrelease profiles. In some instances, the tablets of the instantinvention may be coated, such as with an enteric coating. One of skillin the art will appreciate that other excipients are useful in thetablets of the present invention.

Lozenges useful in the present invention include an appropriate amountof the active agent as well as any fillers, binders, disintegrants,solvents, solubilizing agents, sweeteners, coloring agents and any otheringredients that one of skill in the art would appreciate is necessary.Lozenges of the present invention are designed to dissolve and releasethe active agent on contact with the mouth of the patient. One of skillin the art will appreciate that other delivery methods are useful in thepresent invention.

Formulations of the salts of this invention are prepared for storage oradministration by mixing the salt having a desired degree of purity withphysiologically acceptable carriers, excipients, stabilizers etc., andmay be provided in sustained release or timed release formulations.Acceptable carriers or diluents for therapeutic use are well known inthe pharmaceutical field, and are described, for example, in Remington'sPharmaceutical Sciences, Mack Publishing Co., (A. R. Gennaro Ed. 1985).Such materials are nontoxic to the recipients at the dosages andconcentrations employed, and include buffers such as phosphate, citrate,acetate and other organic acid salts, antioxidants such as ascorbicacid, low molecular weight (less than about ten residues) peptides suchas polyarginine, proteins, such as serum albumin, gelatin, orimmunoglobulins, hydrophilic polymers such as polyvinylpyrrolidinone,amino acids such as glycine, glutamic acid, aspartic acid, or arginine,monosaccharides, disaccharides, and other carbohydrates includingcellulose or its derivatives, glucose, mannose or dextrins, chelatingagents such as EDTA, sugar alcohols such as mannitol or sorbitol,counterions such as sodium, and/or nonionic surfactants such as Tween,Pluronics or polyethyleneglycol.

Dosage formulations of the salts of this invention to be used fortherapeutic administration must be sterile. Sterility is readilyaccomplished by filtration through sterile membranes such as 0.2 micronmembranes, or by other conventional methods. Formulations typically willbe stored in lyophilized form or as an aqueous solution. The pH of thepreparations of this invention typically will be between 3 and 11, morepreferably from 5 to 9 and most preferably from 7 to 8. It will beunderstood that use of certain of the foregoing excipients, carriers, orstabilizers will result in the formation of cyclic polypeptide salts.While the preferred route of administration is by injection, othermethods of administration are also anticipated such as intravenously(bolus and/or infusion), subcutaneously, intramuscularly, colonically,rectally, nasally or intraperitoneally, employing a variety of dosageforms such as suppositories, implanted pellets or small cylinders,aerosols, oral dosage formulations (such as tablets, capsules andlozenges) and topical formulations such as ointments, drops and dermalpatches. The sterile of this invention are desirably incorporated intoshaped articles such as implants which may employ inert materials suchas biodegradable polymers or synthetic silicones, for example, Silastic,silicone rubber or other polymers commercially available.

The salts of the invention may also be administered in the form ofliposome delivery systems, such as small unilamellar vesicles, largeunilamellar vesicles and multilamellar vesicles. Liposomes can be formedfrom a variety of lipids, such as cholesterol, stearylamine orphosphatidylcholines.

The salts of this invention may also be delivered by the use ofantibodies, antibody fragments, growth factors, hormones, or othertargeting moieties, to which the salt molecules are coupled. The saltsof this invention may also be coupled with suitable polymers astargetable drug carriers. Such polymers can includepolyvinylpyrrolidinone, pyran copolymer,polyhydroxy-propyl-methacrylamide-phenol,polyhydroxyethyl-aspartamide-phenol, or polyethyleneoxide-polylysinesubstituted with palmitoyl residues. Furthermore, salts of the inventionmay be coupled to a class of biodegradable polymers useful in achievingcontrolled release of a drug, for example polylactic acid, polyglycolicacid, copolymers of polylactic and polyglycolic acid, polyepsiloncaprolactone, polyhydroxy butyric acid, polyorthoesters, polyacetals,polydihydropyrans, polycyanoacrylates and cross linked or amphipathicblock copolymers of hydrogels. Polymers and semipermeable polymermatrices may be formed into shaped articles, such as valves, stents,tubing, prostheses and the like.

B. Dosing

Typically, about 0.5 to 500 mg of a salt or mixture of salts of thisinvention is compounded with a physiologically acceptable vehicle,carrier, excipient, binder, preservative, stabilizer, dye, flavor etc.,as called for by accepted pharmaceutical practice. The amount of activeingredient in these compositions is such that a suitable dosage in therange indicated is obtained.

It is contemplated that a typical dosage will range from about 0.001mg/kg to about 1000 mg/kg, preferably from about 0.01 mg/kg to about 100mg/kg, and more preferably from about 0.10 mg/kg to about 20 mg/kg. Thecompounds of this invention may be administered once or several timesdaily and other dosage regimens may also be useful.

IV. METHODS

A. Preventing and Treating Disease Conditions Characterized by UndesiredThrombosis

The salt of the present invention can be used for preventing or treatinga condition in a mammal characterized by undesired thrombosis byadministering to the mammal a therapeutically effective amount of a saltof the compound of Formula I, the maleate salt of the compound ofFormula I, the salt of Formula II, or a salt of Formula II having acrystalline polymorph form. The salts can be used either alone or inconjunction with pharmaceutically acceptable excipients to prevent theonset of a condition characterized by undesired thrombosis. Prophylactictreatment can have substantial benefits for a patient at risk of anailment, through decreased medical treatments and their associatedmental and physical costs, as well as the direct monetary savings fromavoiding prolonged treatment of a patient. For patients where thecondition is not detected sufficiently early to prevent onset, the saltof the present invention can be used either alone or in conjunction withpharmaceutically acceptable excipients to treat the condition.

The preferred salts of the present invention are characterized by theirability to inhibit thrombus formation with acceptable effects onclassical measures of coagulation parameters, platelets and plateletfunction, and acceptable levels of bleeding complications associatedwith their use while exhibiting suitable stability. Conditionscharacterized by undesired thrombosis would include those involving thearterial and venous vasculature.

With respect to the coronary arterial vasculature, abnormal thrombusformation characterizes the rupture of an established atheroscleroticplaque which is the major cause of acute myocardial infarction andunstable angina, as well as also characterizing the occlusive coronarythrombus formation resulting from either thrombolytic therapy orpercutaneous transluminal coronary angioplasty (PTCA).

With respect to the venous vasculature, abnormal thrombus formationcharacterizes the condition observed in patients undergoing majorsurgery in the lower extremities or the abdominal area who often sufferfrom thrombus formation in the venous vasculature resulting in reducedblood flow to the affected extremity and a predisposition to pulmonaryembolism. Abnormal thrombus formation further characterizes disseminatedintravascular coagulopathy commonly occurs within both vascular systemsduring septic shock, certain viral infections and cancer, a conditionwherein there is rapid consumption of coagulation factors and systemiccoagulation which results in the formation of life-threatening thrombioccurring throughout the microvasculature leading to widespread organfailure.

The salts of the present invention, selected and used as disclosedherein, are believed to be useful for preventing or treating a conditioncharacterized by undesired thrombosis, such as (a) the treatment of anythrombotically mediated acute coronary syndrome including myocardialinfarction, unstable angina, refractory angina, occlusive coronarythrombus occurring post-thrombolytic therapy or post-coronaryangioplasty, (b) the treatment of any thrombotically mediatedcerebrovascular syndrome including embolic stroke, thrombotic stroke ortransient ischemic attacks, (c) the treatment of any thrombotic syndromeoccurring in the venous system including deep venous thrombosis orpulmonary embolus occurring either spontaneously or in the setting ofmalignancy, surgery or trauma, (d) the treatment of any coagulopathyincluding disseminated intravascular coagulation (including the settingof septic shock or other infection, surgery, pregnancy, trauma ormalignancy and whether associated with multi-organ failure or not),thrombotic thrombocytopenic purpura, thromboangiitis obliterans, orthrombotic disease associated with heparin induced thrombocytopenia, (e)the treatment of thrombotic complications associated with extracorporealcirculation (e.g. renal dialysis, cardiopulmonary bypass or otheroxygenation procedure, plasmapheresis), (f) the treatment of thromboticcomplications associated with instrumentation (e.g. cardiac or otherintravascular catheterization, intra-aortic balloon pump, coronary stentor cardiac valve), and (g) those involved with the fitting of prostheticdevices.

Accordingly, a method for treating a condition in a mammal characterizedby undesired thrombosis comprises administering to the mammal atherapeutically effective amount of a salt of this invention. Diseasestates that are contemplated to be treatable using the salts of thepresent invention include, but are not limited to, acute coronarysyndrome, myocardial infarction, unstable angina, refractory angina,occlusive coronary thrombus occurring post-thrombolytic therapy orpost-coronary angioplasty, a thrombotically mediated cerebrovascularsyndrome, embolic stroke, thrombotic stroke, transient ischemic attacks,venous thrombosis, deep venous thrombosis, pulmonary embolus,coagulopathy, disseminated intravascular coagulation, thromboticthrombocytopenic purpura, thromboanglitis obliterans, thrombotic diseaseassociated with heparin-induced thrombocytopenia, thromboticcomplications associated with extracorporeal circulation, thromboticcomplications associated with instrumentation, thrombotic complicationsassociated with the fitting of prosthetic devices, occlusive coronarythrombus formation resulting from either thrombolytic therapy orpercutaneous transluminal coronary angioplasty, thrombus formation inthe venous vasculature, disseminated intravascular coagulopathy, acondition wherein there is rapid consumption of coagulation factors andsystemic coagulation which results in the formation of life-threateningthrombi occurring throughout the microvasculature leading to widespreadorgan failure, hemorrhagic stroke, renal dialysis, blood oxygenation,and cardiac catheterization.

The maleate salt of the compound of Formula I or the salt of Formula IIcan also be used whenever inhibition of blood coagulation is requiredsuch as to prevent coagulation of stored whole blood and to preventcoagulation in other biological samples for testing or storage. Thuscoagulation inhibitors of the present inhibition can be added to orcontacted with stored whole blood and any medium containing or suspectedof containing plasma coagulation factors and in which it is desired thatblood coagulation be inhibited, e.g. when contacting the mammal's bloodwith material selected from the group consisting of vascular grafts,stents, orthopedic prosthesis, cardiac prosthesis, and extracorporealcirculation systems.

Besides being useful for human treatment, these salts are alsocontemplated to be useful for veterinary treatment of companion animals,exotic animals and farm animals, including mammals, rodents, and thelike. More preferred animals include horses, dogs, and cats.

B. Administration

Therapeutic liquid formulations generally are placed into a containerhaving a sterile access port, for example, an intravenous solution bagor vial having a stopper pierceable by hypodermic injection needle.

Therapeutically effective dosages may be determined by either in vitroor in vivo methods. For each particular salt of the present invention,individual determinations may be made to determine the optimal dosagerequired. The range of therapeutically effective dosages will beinfluenced by the route of administration, the therapeutic objectivesand the condition of the patient. For injection by hypodermic needle, itmay be assumed the dosage is delivered into the body's fluids. For otherroutes of administration, the absorption efficiency must be individuallydetermined for each compound by methods well known in pharmacology.Accordingly, it may be necessary for the therapist to titer the dosageand modify the route of administration as required to obtain the optimaltherapeutic effect. The determination of effective dosage levels, thatis, the dosage levels necessary to achieve the desired result, will bereadily determined by one skilled in the art. Typically, applications ofthe salts are commenced at lower dosage levels, with dosage levels beingincreased until the desired effect is achieved.

Typical adjuvants which may be incorporated into tablets, capsules,lozenges and the like are binders such as acacia, corn starch orgelatin, and excipients such as microcrystalline cellulose,disintegrating agents like corn starch or alginic acid, lubricants suchas magnesium stearate, sweetening agents such as sucrose or lactose, orflavoring agents. When a dosage form is a capsule, in addition to theabove materials it may also contain liquid carriers such as water,saline, or a fatty oil. Other materials of various types may be used ascoatings or as modifiers of the physical form of the dosage unit.Sterile compositions for injection can be formulated according toconventional pharmaceutical practice. For example, dissolution orsuspension of the active compound in a vehicle such as an oil or asynthetic fatty vehicle like ethyl oleate, or into a liposome may bedesired. Buffers, preservatives, antioxidants and the like can beincorporated according to accepted pharmaceutical practice.

C. Combination Therapies

The salts of the present invention may also be used in combination withother therapeutic or diagnostic agents. In certain preferredembodiments, the salts of this invention may be coadministered alongwith other compounds typically prescribed for these conditions accordingto generally accepted medical practice such as anticoagulant agents,thrombolytic agents, or other antithrombotics, including plateletaggregation inhibitors, tissue plasminogen activators, urokinase,prourokinase, streptokinase, heparin, aspirin, or warfarin. The salts ofthe present invention may act in a synergistic fashion to preventreocclusion following a successful thrombolytic therapy and/or reducethe time to reperfusion. These salts may also allow for reduced doses ofthe thrombolytic agents to be used and therefore minimize potentialhemorrhagic side-effects. The salts of this invention can be utilized invivo, ordinarily in mammals such as primates, humans, sheep, horses,cattle, pigs, dogs, cats, rats and mice, or in vitro.

D. Compound Preparation

1. The Maleate Salt of the Compound of Formula I

The compound of Formula I can be converted to salts of various inorganicand organic acids including, but not limited to, HCl salt, lactate,maleate, phenoxyacetate, propionate, succinate, adipate, ascorbate,camphorate, gluconate, phosphate, tartrate, citrate, mesylate, fumarate,glycolate, naphthalene-1,5-disulphonate, gentisate and benzenesulfonate. One of skill in the art will recognize that other acids canbe used to make salts comprising the compound of Formula I that areuseful in the present invention. It is also contemplated that salts ofthe invention can be readily converted to other salts of the invention.

To assess the thermal and hydrolytic stability of the salt, tests knownto those of skill in the art are performed. These tests are morethoroughly discussed in Example 4 below.

A number of methods are useful for the preparation of the saltsdescribed above and are known to those skilled in the art. For example,reaction of the compound of Formula I with one or more molar equivalentsof the desired acid in a solvent or solvent mixture in which the salt isinsoluble, or in a solvent like water after which the solvent is removedby evaporation, distillation or freeze drying. Alternatively, thecompound of Formula I may be passed over an ion exchange resin to formthe desired salt or one salt form of the product may be converted toanother using the same general process.

The compound of Formula I was prepared according to the procedure setforth below. The maleate salt of the compound of Formula I was chosenfor its excellent crystallinity, thermal and hydrolytic stability, andhigh purity.

2. Formula I

The compound of Formula I can be prepared according to any of severaldifferent methodologies, either on a gram scale (<1 kg) or a kilogramscale (>1 kg). A gram-scale method is set forth below in Example 2.Another gram-scale method is set forth in U.S. Pat. No. 6,844,367B1, seeExample 266, which is hereby incorporated by reference.

Alternatively, the compound of Formula I can be prepared on a kilogramscale using the procedure set forth in Example 2. The formation of thedimethyl amidine of Formula I involves nucleophilic attack on a cyanogroup by a deprotonated amine, with the deprotonated amine formed from asecondary amine and an alkyl lithium. As used herein, the term “alkyl”refers to a hydrocarbyl radical of from 1 to 8 carbon atoms. One ofskill in the art will recognize that the deprotonated amine can beformed via other methods, and formation of the amidine functionality ofFormula I can be prepared by a variety of other methods.

A useful solvent for the method of the present invention as describedabove is a non-polar, aprotic solvent such as tetrahydrofuran (THF),diethyl ether, dimethoxymethane, dioxane, hexane, methyl tert-butylether, heptane, and cyclohexane. In addition, the formation of thedeprotonated amine can be carried at temperatures below 10° C. Thenucleophilic addition of the amine to form the compound of Formula I canalso be carried out at temperatures below 10° C. One of skill in the artwill recognize that the methods of the present invention can bepracticed using various other solvents, reagents, and reactiontemperatures.

The compound of Formula I can be prepared using the method of thepresent invention in yields greater than 50%. In some instances, thecompound of Formula I can be prepared in yields greater than 65%. Inother instances, the compound of Formula I can be prepared in yieldsgreater than 75%.

In addition while the method of the present invention for preparing thecompound of Formula I on a gram-scale is similar to the procedure usedon the kilogram-scale, there is an increase in the scale of the reactionof more than 3400%. Moreover, in several steps increased yields areobtained using reduced amounts of the excess reagents. One of skill inthe art will recognize that the compound of Formula I can be preparedvia other chemical methodologies on both a gram and kilogram scale.

V. EXAMPLES

Unless stated otherwise, the abbreviations used throughout thespecification have the following meanings:

Å=Angstrom

A %=total percent area

aq.=aqueous

cm=centimeter

d=doublet

DSC=differential scanning calorimetry

EDTA=ethylenediaminetetraacetic acid

eq. equivalent

EtOH=ethanol

g=gram

HPLC=high performance liquid chromatography

hr=hour

Hz=Hertz

IR=infrared

J=coupling constant

kg=kilogram

kV=killivolts

L=liter

LOD=limit of detection

M=molar

m=multiplet

mA=milliampere

Me=methyl

MeO=methoxy

MeOH=methanol

mg=milligram

min.=minute

mL=milliliter

mm=millimeter

MTBE=methyl tert-butyl ether

N=normal

nM=nanomolar

NMR=nuclear magnetic resonance

s=singlet

TDS=total dissolved solids

TGA=thermal gravimetric analysis

THF=tetrahydrofuran

μM=micromolar

Example 1 Preparation of a Crystalline Polymorph Salt of Formula II

Gram Scale Preparation

In a 3-necked 1500 mL round bottomed flash equipped with a condenser,free base compound of Formula I (25 g; 1 eq.) was charged and 9:1EtOH/Water (500 mL) was added while stirring. The resulting slurry washeated to 70° C. Maleic acid (12.77 g; 2 eq.) was added dropwise as asolution (100 mL of 9:1 EtOH/Water) and after 50 mL had been added, thesolution became noticeably clearer. On complete addition of the maleicacid solution, the temperature was held at 80° C. for 5 minutes. Thevessel was allowed to cool slowly to 45° C. and 400 mL of MTBE was thenadded. The solution was stirred for 12 hr. The resulting precipitate wasfiltered and dried under vacuum. The salt of Formula II was recovered ina 45% yield (14.2 g).

Kilogram Scale Preparation

The compound of Formula I (24.6 Kg) was charged into a 760 L GLMSreactor (Reactor A). Maleic acid (12.7 Kg, 2.0 eq), ethanol (445 Kg,18.1 parts), and high purity water (140 Kg, 5.7 parts) were added. Thereaction mixture was adjusted to 22° C. (19 to 25° C.) and agitated atthat temperature for ca. 1 hr, then transferred through a polishingfilter into a conditioned 780 L Hastelloy reactor (Reactor B). TheReactor A pump and lines were rinsed forward into Reactor B withadditional ethanol (ca. 45 Kg) via polishing filter. The filtrate wasconcentrated under vacuum with a maximum temperature of warm glycol bath(to heat reactor jacket) of 45° C., until ca. 140 L (5.7 parts volume)remained. The Reactor B contents were sampled for in-process NMR, whichshowed that mole ratio of ethanol:Formula II was 26. High purity water(49 Kg, 2.0 parts) was charged to Reactor B and concentration undervacuum resumed until a pot volume of ca. 140 L (5.7 parts volume) wasachieved. In-process NMR indicated that the mole ratio of ethanol:saltof Formula II was 14. High purity water (49 Kg, 2.0 parts) was againcharged and concentration under vacuum resumed to obtain a pot volume ofca. 140 L. In-process NMR showed that the mole ratio ethanol:salt ofFormula II was 5. The temperature of the Reactor B contents wereadjusted to 22° C. (19 to 25° C.) and formation of a slurry was visuallyconfirmed. The reaction mixture was agitated at 22° C. (19 to 25° C.)for ca. 2 hrs, and then filtered onto a 30″ centrifuge fitted with F-53filter cloth. The Reactor B pump and lines were rinsed forward to the30″ centrifuge via polishing filter with two portions of high puritywater (ca. 30 Kg each). The filter cake was sampled for in-process HPLC,which showed that the purity of the product was 99.1 A %, the largestimpurity was 0.26 A %, and therefore recrystallization was unnecessary.The filter cake (33.1 Kg) was dried under vacuum with a maximumtemperature of warm glycol bath (to heat reactor jacket) of 40° C. Afterca. 30.5 hrs, in-process LOD analysis indicated a solvent content of 0%.The dry product was discharged (26.4 Kg) and stored at 2-8° C. The yieldfor the final product was slightly higher than expected at 85% (expected50-80%).

The salt of Formula II was characterized using the techniques describedin Example 4. The X-ray diffraction pattern for the salt of Formula IIis shown in FIG. 1A, and is characterized by the following approximatepeak locations: 4.9, 9.7, 11.8, 13.8, 14.1, 15.2, 17.6, 18.5, 19.9,20.8, 21.6, 22.7, 24.1, 25.0, 26.3, 26.8 degrees 2θ. A melting point ofbetween 197 and 201° C. was measured using differential scanningcalorimetry (DSC, see pattern in FIG. 2A). In addition, a weight loss of0.62% at 100° C. of the salt of Formula II was measured via thermalgravimetric analysis (TGA, see pattern in FIG. 2B). Water sorption ofthe salt of Formula II was reversible and showed a water uptake ofbetween 0.1 and 3% (FIG. 3). Purity of the salt of Formula II wasmeasured by the presence of hydrolyzed amidine content as measured byHPLC, and the purity was found to be >99%.

¹H NMR (DMSO-d₆): δ 3.0 (s, 3H), 3.2 (s, 3H), 3.82 (s, 3H), 7.2 (d, 1H,J=9.0 Hz), 7.42 (s, 1H), 7.68 (d, 1H, J=8.0 Hz), 7.95-8.15 (m, 2H), 8.12(m), 8.18(m, 1H), 8.42 (s, 1H), 9.0 (s, 1H), 11.0 (s, 1H), 11.2 (s, 1H);IR (KBr, cm⁻¹): 3300, 1685, 1600 1515, 1380, 1270, 1200, 1100, 1050,880, 800, 710.

Example 2 Preparation of the Compound of Formula I

Gram Scale Preparation

A slurry of the compound of Formula F (455 g, 1.0 eq.) in THF (4.67 kg,10.3 parts) was prepared and adjusted to <10° C. Lithium dimethyl amidewas prepared as follows; hexyllithium (2.3 N/hexane, 2.45 L, 5.5 eq.)was added to dimethylamine solution (2 N/THF, 2.8 L, 5.5 eq.)maintaining <10° C. The lithium dimethyl amide solution was charged intothe slurry containing the compound of Formula F keeping the pottemperature of <10° C. The reaction progress was monitored by in-processHPLC which confirmed that the amount of Formula F was <1.0 A %. A buffersolution of NaHCO₃ (490 g, 1.1 parts, 5.7 eq.) and Na₂CO₃ (490 g, 1.1parts, 4.5 eq.) in deionized water (6.6 kg, 14.51 parts) was prepared,and above reaction mixture was transferred to this aqueous solutionmaintaining <5° C. The product precipitated out and the resulting slurrywas adjusted to 20° C. over a period of 12 hr. The solid was filtered,and the resulting wet cake was washed with 3.5 kg (7.7 parts) ofdeionized water. The solid was filtered off using a coarse frit glassbench filter, and rinsed forwarded with cold (0-5° C.) absolute ethanol(628 g, 1.4 parts). The product was dried at 30-35° C. Dry product wasobtained in 458 g (73% yield).

Kilogram Scale Preparation

A slurry of the compound of Formula F (31.5 Kg, 1.0 eq) in THF (251 Kg,8.0 parts) was prepared in a 780 L Hastelloy reactor (Reactor A) andadjusted to 0° C. (−3 to 3° C.). 2 M Dimethylamine in THF (161.0 Kg, 5.0eq) and THF (63 Kg, 2 parts) were charged into a 1900 L GLMS reactor(Reactor B) and adjusted to 0° C. (−3 to 3° C.) with maximum agitation.Hexyllithium (2.3 M, 97.2 Kg, 4.5 eq) was slowly charged to Reactor Bwhile maintaining a max temperature of 10° C. The pump and lines wererinsed forward to Reactor B with THF (3.2 Kg). The Reactor B contentswere adjusted to 0° C. (−3 to 3° C.), then transferred to Reactor Awhile keeping Reactor A temperature ≦10° C. The Reactor B pump and lineswere rinsed forward with THF (31.4 Kg, 1.0 part). The Reactor A contentswere adjusted to 0° C. (−3 to 3° C.), and agitated at this temperatureuntil the reaction was complete as verified by HPLC (1-2 hrs). Afterabout 1 hr of agitation, in-process HPLC analysis indicated that 0 A %starting material remained (in-process criteria: max 1 A %). Reactor Acontents were adjusted to −5° C. (−8 to −3° C.). In-process cleaning ofReactor B with water was performed. Two previously prepared aqueoussolutions [NaHCO₃ (35.0 Kg, 1.1 parts) in water (236 Kg, 7.5 parts), andNa₂CO₃ (35.0 Kg 1.1 parts) in water (236 Kg, 7.5 parts)] were charged toReactor B and adjusted to −3° C. (0 to 6° C.). Reactor A contents weretransferred to Reactor B through an insulated line, maintaining thetemperature of Reactor B at −8° C. to a maximum of 5° C. The Reactor Apump and lines were rinsed forward with cold [−5° C. (−8 to −3° C.)] THF(31.4 Kg, 1.0 part). Reactor B contents were adjusted to 22° C. (19 to25° C.) and agitated for ca. 3 hrs. Slurry formation was visuallyconfirmed, and Reactor B contents were filtered onto a 30″ centrifugefitted with F-16 filter cloth. The Reactor B pump and lines were rinsedforward onto the 30″ centrifuge fitted with F-16 filter cloth withdrinking water (63 Kg, 2 parts). The wet filter cake (66.5 Kg) wastransferred back to Reactor B and submitted to a slurry wash in drinkingwater (1005 Kg, 32 parts) at 22° C. (19 to 25)° C. for ca. 1 hr. Theproduct was filtered onto the 30″ centrifuge (after in-process cleaningand fitting with F-53 filter cloth), and the Reactor B lines and pumpwere rinsed forward with drinking water (63 Kg, 2 parts). The waterrinse was sampled for test by TDS, which was found to be 0.46%. TheReactor B pump, lines and wet filter cake were further rinsed with cold[0° C. (−3 to 3° C.)] ethanol (44 Kg, 1.39 parts). The wet filter cakewas dried under vacuum with a maximum temperature of water bath (to heatreactor jacket) of 35° C. In-process LOD was 0% after ca. 24 hrs ofdrying, and the product was discharged (24.8 Kg) in 76.7% yield. HPLCshowed 98% purity, with dechlorinated impurity at 1.14%.

Example 3 Preparation of the Compound of Formula F Step 1. Synthesis of2-nitro-N-(5-chloro-pyridin-2-yl)-5-methoxy-benzamide (C)

5-Methoxy-2-nitrobenzoic acid (A) (25.0 Kg, 1.0 eq),2-amino-5-chloropyridine (B) (16.3 Kg, 1.0 eq), and acetonitrile (87.5Kg, 3.5 parts) were charged to a 380 L GLMS reactor. The reactionmixture was adjusted to 22° C. (19 to 25° C.) and anhydrous pyridine(30.0 Kg, 3.0 eq) was added. The pump and lines were rinsed forward withacetonitrile (22.5 Kg, 0.9 parts), and the reactor contents wereadjusted to a temperature of 19-22° C. Phosphorous oxychloride (23.3 Kg,1.20 eq) was charged to the contents of the reactor via a metering pump,while maintaining a temperature of 25° C. (22-28° C.). The metering pumpand lines were rinsed forward with acetonitrile (12.5 Kg, 0.5 parts),while keeping the temperature at 25° C. (22-28° C.). The reactionmixture normally turned from a slurry to a clear solution after theaddition of about ⅓ of the POCl₃. At the end of the addition, it becameturbid. After complete addition, the reaction mixture was agitated at25° C. (22-28° C.) for ca. 1 hr, at which time HPLC analysis confirmedreaction completion. The solution was cooled to 15° C. (12-18° C.) anddrinking water (156.3 Kg, 6.25 parts) was charged slowly while keepingreaction temperature between 12 and 30° C. The reaction mixture was thenadjusted to 22° C. (19 to 25° C.) and agitated for ca. 5 hrs untilexotherm ceased. Formation of a slurry was visually confirmed and thecontents of the reactor were filtered onto a pressure nutsche fittedwith F-19 filter cloth. The reactor, pump, and lines were washed forwardonto the pressure nutsche with two portions of drinking water (62.5 Kg,2.5 parts each). The filtrate had a pH value of 7. The product (41.8 Kg)was dried under vacuum with a maximum temperature of water bath (to heatreactor jacket) of 50° C. After ca. 12 hrs, in-process LOD analysisindicated a solvent content of 0.72%. The dry product (C) was discharged(34.4 Kg) with 88.2% yield and 99.1% purity by HPLC.

Step 2. Synthesis of2-amino-N-(5-chloro-pyridin-2-yl)-5-methoxy-benzamide (D)

To a 780 L Hastelloy reactor, compound C (33 Kg, 1.0 eq), 5% platinumcarbon (sulfided, 0.33 Kg, 0.010 parts) and dichloromethane (578 Kg,17.5 parts) were charged. Agitation was started and reactor contentswere adjusted to 22° C. (19 to 25° C.). The reactor was pressurized withca. 30 psi hydrogen and the reaction mixture gently heated to 28° C.(25-31° C.). Hydrogenation of the reactor contents was performed underca. 30 psi at 28° C. (25 to 31° C.; maximum 31° C.) until the reactionwas complete by HPLC. After 16.5 hrs, the reaction was deemed completeafter confirming the disappearance of starting material (0.472 A %). Thecontents of the reactor were circulated through a conditioned celite pad(0.2-0.5 Kg celite conditioned with 20-55 Kg dichloromethane) preparedin a 8″ sparkler filter to remove the platinum catalyst. The reactor andcelite bed were rinsed forward with two portions of dichloromethane (83Kg, 2.5 parts each). The filtrate was transferred to and concentrated ina 570 L GLMS reactor under a atmospheric pressure to ca. 132 L (4 partsvolume). Ethanol (69 Kg, 2.1 parts) was charged and concentrationcontinued under atmospheric pressure to ca. 99 L (3 parts volume).In-process NMR indicated that the dichloromethane content was 39%.Ethanol (69 Kg, 2.1 parts) was charged again and concentration continuedagain to ca. 99 L (3 parts volume). In-process NMR indicated that thedichloromethane content was 5%. The reaction mixture was then adjustedto 3° C. (0 to 6° C.), agitated for ca. 1 hr, and the resulting slurryfiltered onto a jacketed pressure nutsche fitted with F-19 filter cloth.The reactor, pump, and lines were rinsed forward with cold [3° C. (0-6°C.)] ethanol (26 Kg, 0.8 parts). The wet filter cake (36.6 Kg) was driedunder vacuum at 40-50° C. with a maximum temperature of water bath (toheat reactor jacket) of 50° C. LOD analysis after 12.5 hrs indicatedsolvent content was at 0.1%. The dry product (D) was discharged (26.4Kg) in 89.5% yield. HPLC showed 98.4 A % purity, with dechlorinatedimpurity at 0.083%.

Step 3. Synthesis ofN-(5-chloro-pyridin-2-yl)-2-(4-cyano-benzoyl-amino)-5-methoxy-benzamideHydrochloride (F)

To a 780 L Hastelloy reactor, was charged 4-cyanobenzoyl chloride (E)(17.2 Kg, 1.1 eq) and THF (92 Kg, 3.5 parts). Reactor contents wereagitated at 22° C. (19 to 25° C.) until all of the solids had dissolved.The resulting solution was transferred to a lower receiver and thereactor was rinsed forward with THF (26 Kg, 1 part). Compound D (26.4Kg, 1 eq), THF (396 Kg, 15 parts) and pyridine (2.90 Kg, 0.4 eq) werecharged to a clean reactor. The pump and lines were rinsed forward withTHF (34 Kg, 1.3 parts). Via a metering pump, the 4-cyanobenzoylchloride/THF solution was charged to the reactor, keeping thetemperature at ≦30° C. and rinsing forward with THF (ca. 10 Kg). Theresulting yellow-colored slurry was agitated at 22° C. (19 to 25° C.)for ca 2 hrs. In-process HPLC taken after 2 hrs showed a compound ofFormula D content of 0%, indicating completion of the reaction. Theslurry was filtered onto a pressure nutsche fitted with F-19 filtercloth. The reactor, pump, lines, and wet cake were rinsed with threeportions of ethanol (ca. 15 Kg each). The wet filter cake was discharged(65.4 Kg) and transferred back to the reactor for slurry wash in ethanol(317 Kg, 12 parts) at 22° C. (19 to 25° C.) for ca. 1 hr. The slurry wasfiltered onto the pressure nutsche and the reactor, pump, lines, and wetfilter cake were rinsed with two portions of ethanol (ca. 15 Kg each)and two portions of THF (ca. 15 Kg each). The wet filter cake was driedunder vacuum with a maximum temperature of warm glycol bath (to heat thereactor jacket) of 40° C. After 14.5 hrs of drying, LOD was 0.75%. Thedried material was milled (screen 0.125″) to give 31.8 Kg of product,which was dried under vacuum for another 10.5 hrs. LOD after drying was1.8%, and the product was discharged (31.5 Kg) in 74.8% yield (expected60-90%). HPLC showed 100% purity.

Example 4 Salt Screens

Primary Screen

To 20 mg of the free base in 3 mL of 10% (aq.) THF mixture was added 1.1eq. of the acid in 1 mL ethanol. The mixture was shaken for 2 hours,followed by the addition of 2 mL of tert-butyl methyl ether in order toinduce precipitation and shaken for another 2 hours. The samples werethen filtered, dried and then analyzed to judge their purity,crystallinity and stability. The results are presented in Table 1 belowand list the acid tested. TABLE 1 Acid Salt Hydrochloric +++ Lactic +++Maleic +++ Phenoxyacetic +++ Propionic +++ Succinic +++ Adipic ++Ascorbic ++ Camphoric ++ Gluconic ++ Phosphic ++ Tartric ++ Citric ++Methanesulfonic ++ Fumaric + Glycolic + Naphthalene-1,5-disulfonic +Gentisic + Benzene sulfonic + Camphor sulfonic − α-Hydroxycaproic −Benzoic − Glucuronic − Ketoglutaric − Malonic − Mandelic − Pyroglutamic− Sulfuric − trans-Cinnamic −+++, crystalline form, no phase change, good purity;++, amorphous, some phase change, moderate to good purity;+, little or no crystallinity, phase change to less crystalline form,low purity;−, no precipitationSecondary Screen

A secondary evaluation of several salt forms was carried out using themethods described below with the results summarized in the Table 5 andFIGS. 1A, 1B, 2A, 2B and 3.

Differential Scanning Calorimetry (DSC)

DSC data were collected on a TA instrument Q1000 equipped with a 50position autosampler. The energy and temperature calibration standardwas indium. Samples were heated at a rate of 10° C./min between 25 and350° C. A nitrogen purge at 30 mL/min was maintained over the sample.Between 1 and 3 mg of sample was used, unless otherwise stated, and allsamples were crimped in a hermetically sealed aluminium pan.

Thermogravimetric Analysis (TGA)

TGA data were collected on a TA Instrument Q500 TGA, calibrated withNickel/Alumel and running at scan rates of 10° C./minute. A nitrogenpurge at 60 mL/min was maintained over the sample. Typically 10-20 mg ofsample was loaded onto a pre-tared platinum crucible.

XRPD (X-Ray Powder Diffraction)

X-Ray Powder Diffraction patterns were collected on a Siemens D5000diffractometer using CuKα radiation (40 kV, 40 mA), θ-θ goniometer,automatic divergence and receiving slits, a graphite secondarymonochromator and a scintillation counter. The instrument is performancechecked using a certified Corundum standard (NIST 1976).

Samples run under ambient conditions were prepared as flat platespecimens using powder. Approximately 35 mg of the sample was gentlypacked into a cavity cut into polished, zero-background (510) siliconwafer. The sample was rotated in its own plane during analysis. Thedetails of the data collection are given for the method in Table 2below: TABLE 2 XRPD Method Angular range 3°-40° 2θ Step size 0.02° 2θCount time 6 seconds/step Divergence slit V20 Anti-scattering slit V20

Diffraction data are reported using Cu Kα₁ (λ=1.5406 Å), after the Kα₂component had been stripped using EVA (evaluation software), the powderpatterns were indexed by the ITO method using WIN-INDEX and the rawlattice constants refined using WIN-METRIC.

Single Crystal XRD (X-Ray Diffraction)

Data were collected on a Bruker AXS 1K SMART CCD diffractometer equippedwith an Oxford Cryosystems Cryostream cooling device. Structures weresolved using either the SHELXS or SHELXD programs and refined with theSHELXL program as part of the Bruker AXS SHELXTL suite. Unless otherwisestated, hydrogen atoms attached to carbon were placed geometrically andallowed to refine with a riding isotropic displacement parameter.Hydrogen atoms attached to a heteroatom were located in a differenceFourier synthesis and were allowed to refine freely with an isotropicdisplacement parameter.

Gravimetric Vapour Sorption (GVS) Studies

All samples were run on a Hiden IGASorp moisture sorption analyzerrunning CFRSorp software. Sample sizes were typically 10 mg. A moistureadsorption desorption isotherm was performed as outlined below (2 scansgiving 1 complete cycle). All samples were loaded/unloaded at typicalroom humidity and temperature (40% RH, 25° C.). All samples wereanalyzed by XRPD post GVS analysis. The standard isotherm was performedat 25° C. at 10% RH intervals over a 0-90% RH range. The salt of formulaII showed excellent moisture stability.

Solubility

This was measured by suspending enough salt in 0.25 mL of solvent(water) to give a maximum final concentration of ≧10 mg/mL of the parentfree form of the salt. The suspension was equilibrated at 25° C. for 24hr followed by a pH check and filtration through a glass fibre C 96 wellplate. The filtrate was then diluted down 101×. Quantitation was by HPLCwith reference to a standard dissolved in DMSO at approx 0.1 mg/mL.Different volumes of the standard, diluted and undiluted tests wereinjected. The solubility was calculated by integration of the peak areafound at the same retention time as the peak maximum in the standardinjection. If there was sufficient solid in the filter plate the XRPDwas normally checked for phase changes, hydrate formation,amorphization, crystallization, etc.

Acetate salts provided a solubility of ≧10 mg/mL, while the maleatesalts provided a solubility of about 2.05 mg/mL to about 2.27 mg/mL.

pKa Determination

This was performed on a Sirius GlpKa instrument with a D-PAS attachment.Measurements were made by UV in aqueous and by potentiometric inmethanol and water mixtures at 25° C. The titration media was ionicstrength adjusted with 0.15 M KCl. The values found in the methanol andwater mixtures were corrected to 0% co-solvent via a Yasuda-Shedlovskyextrapolation. The data was refined using Refinement Pro softwareversion 1.0. Prediction of pKa values was made using ACD pKa predictionsoftware Ver. 8.08. The data for the salt of formula II is presentedbelow in Table 3. TABLE 3 Compound Predicted/Measured pKa Assignment

ACD predicted Measured 11.91 ± 0.50 11.45 Basic —

ACD Predicted Measured 11.00 ± 0.70 10.90 Acidic —

ACD Predicted Measured  0.57 ± 0.29 1.2 Basic Basic

LogP Determination

This was by potentiometric titration on a Sirius GlpKa instrument usingthree ratios of Octanol:ISA water to generate Log P, Log P_(ion), andLog D values. The data was refined using Refinement Pro software version1.0. Predictions of LogP were made using ACD Ver. 8.08 and SyracuseKNOWWIN Ver. 1.67 software. The data for the maleate salt is shown inTable 4 below. TABLE 4 LogP ACD Predicted LogP 2.93 Syracuse PredictedLogP 3.86 Measured LogP 3.09 Measured LogP_(ion) −0.08 Measured LogD0.09

Karl Fisher Water Determination

Water contents were measured on a Mettler Toledo DL39 Coulometer usingHydranal Coulomat AG reagent and an Argon purge. Samples were introducedinto the vessel as solids weighed out onto a platinum TGA pan which wasconnected to a subaseal to avoid water ingress. Approximately 10 mg ofsample was used per titration and each analysis was performed induplicate.

Stability

As a measure of the stability, the hydrolyzed amidine content wasmeasured by HPLC (Agilent HP1100) (retention time of 34 minutes) aftersubjecting the sample to a temperature of 57° C. with 75% room humidity.The sample solvent was methanol and a mobile phase modifier of 0.1%trifluoroacetic acid was employed. Data were collected after 3, 6 and 10days except data for the propionate was collected at 0, 3, and 8 days.The results are presented in Table 5 as a percentage of the acidhydrolysis product, expressed as a percentage of the main peak. Allother impurity peaks were disregarded in the calculation TABLE 5Hydrolyzed Hydrolyzed Hydrolyzed DSC Amidine Amidine Amidine meltingWater Content Content Content Salt Crystallinity point Sorption (3 days)(6 days) (10 days) Acetate crystalline — non- 0.62-1.11% 2.30-3.56%3.61-7.90% reversible, high uptake (40%) HCl salt amorphous — — — — —Succinate amorphous — — — — — Citrate amorphous — — 2.06% 2.36% 2.68%Lactate part multiple — — — — crystalline events Maleate crystalline197-201° C. reversible,  0.0%  0.0%  0.0% low uptake (0.1-3%)Phenoxyacetate part multiple — — — — crystalline events Propionatecrystalline 129, reversible, 2.22% 2.97% 1.71% 253° C. medium uptake(3.1%) Mesylate crystalline multiple — — — — events Pamoate/ crystalline— — — — — Embonate Adipate part multiple — — — — crystalline eventsAscorbate — — — — — — Camphorate crystalline multiple — — — — eventsGluconate — — — — — — Phosphate part multiple — — — — crystalline eventsTartrate amorphous multiple — — — — events

Crystal Data for the Salt of Formula II

All experiments are performed on a Bruker-Nonius Kappa CCDdiffractometer equipped with an Oxford Cryosystems Cryostream coolingdevice Structures are usually solved with either SIR-97 or SHELXS-97 andrefined with SHELXL-97. Unless otherwise stated, hydrogen atoms areplaced geometrically and allowed to refine with isotropic displacementparameters. The following tables (Table 6 and Table 7) provides crystaldata and structure refinement for the salt of Formula II. TABLE 6Empirical formula C₂₇H₂₆ClN₅O₇ Formula weight 567.98 Temperature 180(2)K Wavelength 0.71073 Å Crystal size 0.35 × 0.23 × 0.12 mm Crystal habitcolorless block Crystal system Triclinic Space group P1 Unit celldimensions a = 10.3321(2) Å α = 73.1530(10)° b = 14.0715(3) Å β =75.4860(10)° c = 19.5756(5) Å γ = 89.6050(10)° Volume 2630.34(10) Å³ Z 4

TABLE 7 Theta range for data collection 3.53 to 26.37° Coverage ofindependent reflections 99.4% Goodness-of-fit on F² 1.001 Final Rindices R1 = 0.0542, 7196 data; I > 2σ(I) wR2 = 0.1329

Although the foregoing invention has been described in some detail byway of illustration and example for purposes of clarity ofunderstanding, one of skill in the art will appreciate that certainchanges and modifications may be practiced within the scope of theappended claims. In addition, each reference provided herein isincorporated by reference in its entirety to the same extent as if eachreference was individually incorporated by reference.

1. A salt comprising a compound Formula I:

and an acid selected from the group consisting of hydrochloric, lactic,maleic, phenoxyacetic, propionic, succinic, adipic, ascorbic, camphoric,gluconic, phosphic, tartric, citric, methanesulfonic, fumaric, glycolic,naphthalene-1,5-disulfonic, gentisic and benzenesulfonic.
 2. The salt ofclaim 1, wherein the acid selected from the group consisting ofhydrochloric, lactic, maleic, phenoxyacetic, propionic, succinic,adipic, ascorbic, camphoric, gluconic, phosphic, tartric, citric, andmethanesulfonic.
 3. The salt of claim 1, wherein the acid is selectedfrom the group consisting of hydrochloric, lactic, maleic,phenoxyacetic, propionic, and succinic.
 4. The salt of claim 1, whereinthe acid is maleic.
 5. The salt of claim 1, wherein the acid ispropionic.
 6. The salt of claim 4, wherein the salt is represented byFormula II:


7. The salt of claim 6 having a crystalline polymorph form.
 8. The saltof claim 7, having a powder X-ray diffraction pattern having at leastfour approximate characteristic peak locations selected from 4.9, 9.7,13.8, 14.1, 15.2, 17.6, 18.5, 20.8, 21.6, 22.7, 24.1, 26.3, 26.8 degrees2θ.
 9. The salt of claim 7, having a powder X-ray diffraction patternhaving at least eight approximate characteristic peak locations selectedfrom 4.9, 9.7, 11.8, 13.8, 14.1, 15.2, 17.6, 18.5, 19.9, 20.8, 21.6,22.7, 24.1, 25.0, 26.3, 26.8 degrees 2θ.
 10. The salt of claim 7, havinga powder X-ray diffraction pattern approximate to the powder X-raydiffraction pattern shown in FIG.
 1. 11. The salt of claim 7, having adifferential scanning calorimetry approximate to the differentialscanning calorimetry pattern shown in FIG.
 2. 12. A pharmaceuticalcomposition for preventing or treating a condition in a mammalcharacterized by undesired thrombosis comprising a pharmaceuticallyacceptable carrier and a therapeutically effective amount of a salt asin claims 1, 4, 6, or
 7. 13. The pharmaceutical composition of claim 12in tablet form.
 14. The pharmaceutical composition of claim 12 incapsule form.
 15. The pharmaceutical composition of claim 12 in lozengeform.
 16. The pharmaceutical composition of claim 12 in a form suitablefor infusion, injection, or transdermal delivery.
 17. A method forpreventing or treating a condition in a mammal characterized byundesired thrombosis comprising administering to said mammal atherapeutically effective amount of a salt as in claims 1, 4, 6, or 7.18. The method of claim 17, wherein the condition is a member selectedfrom the group consisting of acute coronary syndrome, myocardialinfarction, unstable angina, refractory angina, occlusive coronarythrombus occurring post-thrombolytic therapy or post-coronaryangioplasty, a thrombotically mediated cerebrovascular syndrome, embolicstroke, thrombotic stroke, transient ischemic attacks, venousthrombosis, deep venous thrombosis, pulmonary embolus, coagulopathy,disseminated intravascular coagulation, thrombotic thrombocytopenicpurpura, thromboanglitis obliterans, thrombotic disease associated withheparin-induced thrombocytopenia, thrombotic complications associatedwith extracorporeal circulation, thrombotic complications associatedwith instrumentation, and thrombotic complications associated with thefitting of prosthetic devices.
 19. A method for inhibiting thecoagulation of a blood sample comprising the step of contacting saidsample with said salt as in claims 1, 4, 6, or
 7. 20. A method ofpreparing a compound of Formula I:

comprising contacting LiN(CH₃)₂ with a compound of formula III:

or a salt thereof under conditions to form the compound of Formula I.21. The method of claim 20, wherein the salt of the compound of FormulaIII is the HCl salt.
 22. The method of claim 20, wherein the conditionscomprise using a non-polar, aprotic solvent.
 23. The method of claim 22,wherein the solvent is a member selected from the group consisting oftetrahydrofuran, diethyl ether, dimethoxymethane, dioxane, hexane,methyl tert-butyl ether, heptane, and cyclohexane.
 24. The method ofclaim 20, wherein the conditions comprise performing the method at atemperature of less than 10° C.
 25. The method of claim 20, wherein thecompound of Formula I is afforded in a yield of at least 50%.
 26. Themethod of claim 20, wherein the compound of Formula I is afforded in ayield of at least 65%.
 27. The method of claim 20, wherein the compoundof Formula I is afforded in a yield of at least 75%.
 28. The method ofclaim 20, wherein the compound of Formula I is prepared on a gram scaleor a kilogram scale.